Intraoperative Monitoring to Predict Postoperative Complications After Thyroidectomy
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorCentral Hospital, Nancy, France
About this trial
The goal of this study is to evaluate the role of intraoperative continous and intermittent neuromonitoring and intraoperative parathormone (PTH) to predict postoperative nerve morbidity and hypocalcemia.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
patients scheduled for total thyroidectomy in university of Nancy (University Hospital)
Disqualifiers
refusal to participate
Trial population
All patients scheduled for total thyroidectomy in university of Nancy (University Hospital)
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
intraoperative parathormone values
parathormone in pg/mL
Time frame
intraoperativeSecondary outcomes
1
postoperative hypocalcemia
calcium in mg/L
Time frame
within 1 week after thyroidectomy2
postoperative hypoparathyroidism
parathormone in pg/mL
Time frame
within 1 week after thyroidectomy3
permanent postoperative hypocalcemia
calcium in mg/L
Time frame
at one year after thyroidectomy4
permanent postoperative hypoparathyroidism
parathormone in pg/mL
Time frame
at one year after thyroidectomySponsors and contacts
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Source ClinicalTrials.gov